Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP635449.RAT4I56lQmkKM0uAS6NRq_Hr9sZeoXQbHpj1shZ_ZBeWQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP635449.RAT4I56lQmkKM0uAS6NRq_Hr9sZeoXQbHpj1shZ_ZBeWQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP635449.RAT4I56lQmkKM0uAS6NRq_Hr9sZeoXQbHpj1shZ_ZBeWQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP635449.RAT4I56lQmkKM0uAS6NRq_Hr9sZeoXQbHpj1shZ_ZBeWQ130_provenance.
- NP635449.RAT4I56lQmkKM0uAS6NRq_Hr9sZeoXQbHpj1shZ_ZBeWQ130_assertion description "[Two novel mutations in the POU1F1 gene generate null alleles through different mechanisms leading to combined pituitary hormone deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP635449.RAT4I56lQmkKM0uAS6NRq_Hr9sZeoXQbHpj1shZ_ZBeWQ130_provenance.
- NP635449.RAT4I56lQmkKM0uAS6NRq_Hr9sZeoXQbHpj1shZ_ZBeWQ130_assertion evidence source_evidence_literature NP635449.RAT4I56lQmkKM0uAS6NRq_Hr9sZeoXQbHpj1shZ_ZBeWQ130_provenance.
- NP635449.RAT4I56lQmkKM0uAS6NRq_Hr9sZeoXQbHpj1shZ_ZBeWQ130_assertion SIO_000772 22010633 NP635449.RAT4I56lQmkKM0uAS6NRq_Hr9sZeoXQbHpj1shZ_ZBeWQ130_provenance.
- NP635449.RAT4I56lQmkKM0uAS6NRq_Hr9sZeoXQbHpj1shZ_ZBeWQ130_assertion wasDerivedFrom befree-20150227 NP635449.RAT4I56lQmkKM0uAS6NRq_Hr9sZeoXQbHpj1shZ_ZBeWQ130_provenance.
- NP635449.RAT4I56lQmkKM0uAS6NRq_Hr9sZeoXQbHpj1shZ_ZBeWQ130_assertion wasGeneratedBy ECO_0000203 NP635449.RAT4I56lQmkKM0uAS6NRq_Hr9sZeoXQbHpj1shZ_ZBeWQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP635449.RAT4I56lQmkKM0uAS6NRq_Hr9sZeoXQbHpj1shZ_ZBeWQ130_provenance.